# FDA Inspection 978225 - Ziosoft USA, Inc. - April 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/ziosoft-usa-inc/7d9f27e2-5093-4f5e-b7f2-df44b4b88b33
Source feed: FDA_Inspections

> FDA Inspection 978225 for Ziosoft USA, Inc. on April 28, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 978225
- Company Name: Ziosoft USA, Inc.
- Inspection Date: 2016-04-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ziosoft-usa-inc/f37d616d-c594-4801-99db-ebef6949b314

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7